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1 ; R. balochistanensis has virtually complete fore- and hind limbs.
2          Eml5 transcripts can be detected in fore- and hindbrain structures from embryonic day 13 onw
3 expanded structures in the fat pads of their fore- and hindfeet, but for three centuries these have b
4 ouse cerebellum, midbrain, nasal process and fore- and hindlimb buds.
5                       Using Tbx5 and Tbx4 as fore- and hindlimb field markers, respectively, we have
6              Furthermore, we found that both fore- and hindlimb fields arise gradually during gastrul
7 rebro-olivocerebellar paths originating from fore- and hindlimb motor cortex has implications for the
8 creases in horizontal bar test catalepsy and fore- and hindlimb paw retraction latencies.
9 ud occurs in the anterior mesenchyme of both fore- and hindlimb.
10  specify the differential development of the fore- and hindlimbs are unknown.
11 ages, pectoral and pelvic fins in fishes and fore- and hindlimbs in tetrapods.
12 th and a 30% decrease in inflammation in the fore- and hindlimbs of mdx mice.
13 tensive anterior digit abnormalities of both fore- and hindlimbs, while all double Bmp4(tm1); Alx4(tm
14  distinct structures, such as the vertebrate fore- and hindlimbs.
15 tal digit duplications were seen in both the fore- and hindlimbs.
16  birth, despite the complete absence of both fore- and hindlimbs.
17 so exhibit syndactyly (digit fusions) of the fore- and hindlimbs.
18 phrenic nerve, and the dorsal motor nerve in fore- and hindlimbs.
19                                              Fore- and hindpaw withdrawal latencies from a 30 degrees
20 a-receptors, in adjacent coronal sections in fore- and midbrain and in sagittal sections, were labell
21 O binding to mu-opioid receptors in selected fore- and midbrain regions of chickens subject to varyin
22 tivity was evident in several regions of the fore- and midbrain, in support of putative homologies to
23 thalamus at the expense of the ZLI and other fore- and/or mid-brain regions.
24 ssion of both genes was found in adult mouse fore- but not mid- or hindbrain.
25 ru imposed strong balancing selection on the Fore, essentially eliminating PRNP 129 homozygotes.
26 isorder characterised predominantly by upper(fore) limb defects and heart abnormalities.
27 dermal cell lineages and a gut consisting of fore-, mid- and hindgut.
28 ormation of large hemorrhages throughout the fore-, mid-, and hindbrain by E11.5.
29 nd oligodendrocytes, which populate the host fore-, mid-, and hindbrain.
30  pattern is formed from three broad domains: fore-, mid-, and hindgut that have distinct functional,
31 l breast milk samples, with a gradient from "fore" milk to "hind" milk.
32    Electrical stimulation of the ipsilateral fore- or hindimbs or somatotopically corresponding parts
33 ssion domains in the heart and the exclusive fore- or hindlimb expression of Tbx5 and Tbx4, respectiv
34 o-Ruby or Fluoro-Emerald) were made into the fore- or hindlimb parts of the motor cortex where stimul
35 ding (spino-olivocerebellar) paths targeting fore- or hindlimb-receiving parts of the C1 zone.
36 are, in marked contrast to younger unexposed Fore, predominantly PRNP 129 heterozygotes.
37 isms of aggregate formation have come to the fore, suggesting that nucleation-dependent aggregation m
38  quantum simulators has recently come to the fore: they generally require less memory than their clas
39 usly shown that combining Fourier rebinning (FORE) with 2-dimensional (2D) statistical image reconstr

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